<1,1-D2>-1-chlorohexadecane | 143030-09-5

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 有机氯化物
• 英文名称: <1,1-D2>-1-chlorohexadecane
• 英文别名: [1,1-D2]-1-chlorohexadecane
• CAS: 143030-09-5
• 化学式: C₁₆H₃₃Cl
• 分子量: 262.875
• InChiKey: CLWAXFZCVYJLLM-BPPAMHLBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.71
• 重原子数：
  17.0
• 可旋转键数：
  14.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  0.0
• 氢给体数：
  0.0
• 氢受体数：
  0.0

反应信息

• 作为反应物：
  描述：

  <1,1-D2>-1-chlorohexadecane 在 吡啶 、 氢氧化钾 、 五氯化磷 、 sodium 、 碳酸氢钠 作用下， 以 乙醇 、 水 、 苯 为溶剂， 反应 24.0h， 生成 17β-estradiol-17-<3',3'-D2>stearate
  参考文献：
  名称：

  Mass spectrometric studies on 17β-estradiol-17-fatty acid esters: Evidence for the formation of anion-dipole intermediates

  摘要：

  AbstractThe behaviour towards low collision energy processes (eV range) of [M  H]− prepared under negative ion chemical ionization (NICI) ammonia conditions from 17β‐estradiol‐17‐fatty acid esters has been investigated. From such bifunctional compounds containing two acidic sites (i.e. phenol and ester groups), two isomeric forms (i.e. phenoxide and enolate forms) characterize the [M  H]− ion structures, whose distribution depends on the ion preparation mode. Here NICI (ammonia) provides both phenoxide and enolate forms as the [M  H]− species. This behaviour contrasts with the regioselectivity observed for proton abstraction from phenol under NICI (N2O) and fast atom bombardment conditions. Production of both phenoxide and enolate forms in NICI (ammonia) is demonstrated under NICI (ND3) conditions in which DO‐labelled [Md  H]− enolate ions are produced in a similar yield to unlabelled [Md  D]− phenoxide ions. Collisionally activated dissociation (CAD) spectra of both isomeric deprotonated molecules differ strongly by the presence of two different pairs of complementary daughter ions, suggesting that these ionic species are unconvertible. This is due to a steric hindrance effect on the long‐distance proton transfer. A mechanistic investigation on the formation of fragment ion pairs produced under CAD was performed with various deuterium‐labelled molecules. From these experiments, evidence is provided for molecular isomerizations into ion‐dipole complexes (prior to dissociation) which are structurally dependent on the initial charge location. Direct dissociation of these intermediates competes with the occurrence of exothermic proton transfer(s) yielding the formation of other isomeric intermediate forms. The orientation of these proton transfers is dictated by the relative acidities of both moieties of the complex.

  DOI：

  10.1002/oms.1210270612
• 作为产物：
  描述：

  hexadecan-1,1-d₂-1-ol 在 吡啶 、 氯化亚砜 作用下， 反应 1.0h， 以55%的产率得到<1,1-D2>-1-chlorohexadecane
  参考文献：
  名称：

  Mass spectrometric studies on 17β-estradiol-17-fatty acid esters: Evidence for the formation of anion-dipole intermediates

  摘要：

  AbstractThe behaviour towards low collision energy processes (eV range) of [M  H]− prepared under negative ion chemical ionization (NICI) ammonia conditions from 17β‐estradiol‐17‐fatty acid esters has been investigated. From such bifunctional compounds containing two acidic sites (i.e. phenol and ester groups), two isomeric forms (i.e. phenoxide and enolate forms) characterize the [M  H]− ion structures, whose distribution depends on the ion preparation mode. Here NICI (ammonia) provides both phenoxide and enolate forms as the [M  H]− species. This behaviour contrasts with the regioselectivity observed for proton abstraction from phenol under NICI (N2O) and fast atom bombardment conditions. Production of both phenoxide and enolate forms in NICI (ammonia) is demonstrated under NICI (ND3) conditions in which DO‐labelled [Md  H]− enolate ions are produced in a similar yield to unlabelled [Md  D]− phenoxide ions. Collisionally activated dissociation (CAD) spectra of both isomeric deprotonated molecules differ strongly by the presence of two different pairs of complementary daughter ions, suggesting that these ionic species are unconvertible. This is due to a steric hindrance effect on the long‐distance proton transfer. A mechanistic investigation on the formation of fragment ion pairs produced under CAD was performed with various deuterium‐labelled molecules. From these experiments, evidence is provided for molecular isomerizations into ion‐dipole complexes (prior to dissociation) which are structurally dependent on the initial charge location. Direct dissociation of these intermediates competes with the occurrence of exothermic proton transfer(s) yielding the formation of other isomeric intermediate forms. The orientation of these proton transfers is dictated by the relative acidities of both moieties of the complex.

  DOI：

  10.1002/oms.1210270612